首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >An ordered, nonredundant library of Pseudomonas aeruginosa strain PA14 transposon insertion mutants
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An ordered, nonredundant library of Pseudomonas aeruginosa strain PA14 transposon insertion mutants

机译:铜绿假单胞菌菌株PA14转座子插入突变体的有序非冗余文库

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摘要

Random transposon insertion libraries have proven invaluable in studying bacterial genomes. Libraries that approach saturation must be large, with multiple insertions per gene, making comprehensive genome-wide scanning difficult. To facilitate genomescale study of the opportunistic human pathogen Pseudomonas aeruginosa strain PA14, we constructed a nonredundant library of PA14 transposon mutants (the PA14NR Set) in which nonessential PA14 genes are represented by a single transposon insertion chosen from a comprehensive library of insertion mutants. The parental library of PA14 transposon insertion mutants was generated by using MAR2xT7, a transposon compatible with transposonsite hybridization and based on mariner. The transposon-site hybridization genetic footprinting feature broadens the utility of the library by allowing pooled MAR2xT7 mutants to be individually tracked under different experimental conditions. A public, internet-accessible database (the PA14 Transposon Insertion Mutant Database, http://ausubellab.mgh.harvard.edu/cgi-bin/pa14/ home.cgi) was developed to facilitate construction, distribution, and use of the PA14NR Set. The usefulness of the PA14NR Set in genome-wide scanning for phenotypic mutants was validated in a screen for attachment to abiotic surfaces. Comparison of the genes disrupted in the PA14 transposon insertion library with an independently constructed insertion library in A aeruginosa strain PAO1 provides an estimate of the number of P. aeruginosa essential genes.
机译:事实证明,随机转座子插入文库在研究细菌基因组中具有无价的价值。接近饱和的文库必须很大,每个基因有多个插入片段,这使得全面的全基因组扫描变得困难。为了促进对机会性人类病原体铜绿假单胞菌菌株PA14的基因组规模研究,我们构建了PA14转座子突变体(PA14NR集)的非冗余文库,其中非必需的PA14基因由单个转座子插入代表,该插入子选自完整的插入突变体文库。 PA14转座子插入突变体的亲本文库是使用MAR2xT7(与转座子杂交兼容的转座子,基于水手)生成的。转座子位点杂交的遗传足迹特征通过允许在不同的实验条件下单独跟踪合并的MAR2xT7突变体,拓宽了文库的用途。开发了一个公共的,可通过互联网访问的数据库(PA14转座子插入突变体数据库,http://ausubellab.mgh.harvard.edu/cgi-bin/pa14/home.cgi),以促进PA14NR的构建,分发和使用。组。 PA14NR Set在表型突变体的全基因组扫描中的有用性已在非生物表面附着筛选中得到验证。铜绿假单胞菌菌株PAO1中PA14转座子插入文库中破坏的基因与独立构建的插入文库的比较提供了铜绿假单胞菌必需基因数的估计。

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